(R)-2-([2,2'-Bipyridin]-6-yl)-4-(tert-butyl)-4,5-dihydrooxazole

97% 99%ee

Reagent Code: #231382
fingerprint
CAS Number 2757082-47-4

science Other reagents with same CAS 2757082-47-4

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transition metal-catalyzed reactions. It plays a key role in promoting high enantioselectivity in transformations such as asymmetric C–H activation, cross-coupling, and cyclization reactions. Its rigid oxazoline-bipyridine framework enhances metal coordination and stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly employed with palladium, nickel, or copper complexes to achieve efficient asymmetric induction under mild reaction conditions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,940.00
inventory 1g
10-20 days ฿25,320.00
inventory 250mg
10-20 days ฿7,290.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-2-([2,2'-Bipyridin]-6-yl)-4-(tert-butyl)-4,5-dihydrooxazole
No image available

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transition metal-catalyzed reactions. It plays a key role in promoting high enantioselectivity in transformations such as asymmetric C–H activation, cross-coupling, and cyclization reactions. Its rigid oxazoline-bipyridine framework enhances metal coordination and stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly employed with palladium, nickel, or copper com

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transition metal-catalyzed reactions. It plays a key role in promoting high enantioselectivity in transformations such as asymmetric C–H activation, cross-coupling, and cyclization reactions. Its rigid oxazoline-bipyridine framework enhances metal coordination and stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly employed with palladium, nickel, or copper complexes to achieve efficient asymmetric induction under mild reaction conditions.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...